- SR1078
SR3335RORα agonist,partial inverse and selective |
Sample solution is provided at 25 µL, 10mM.
Quality Control & MSDS
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- Purity = 99.52%
- COA (Certificate Of Analysis)
- HPLC
- NMR (Nuclear Magnetic Resonance)
- MSDS (Material Safety Data Sheet)
- Datasheet
Chemical structure
Description | SR3335 is a selective inverse agonist of retinoic acid receptor-related orphan receptor (ROR) RORα with IC50 value of 480 nM. | |||||
Targets | RORα | |||||
IC50 | 480 nM |
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Cas No. | 293753-05-6 | SDF | Download SDF |
Synonyms | ML-176;SR 3335;SR-3335;ML176;ML 176 | ||
Chemical Name | N-[4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl]thiophene-2-sulfonamide | ||
Canonical SMILES | C1=CSC(=C1)S(=O)(=O)NC2=CC=C(C=C2)C(C(F)(F)F)(C(F)(F)F)O | ||
Formula | C13H9F6NO3S2 | M.Wt | 405.34 |
Solubility | ≥88.8 mg/mL in DMSO, ≥87.4 mg/mL in EtOH, <2.07 mg/ml="" in="" h2o="">2.07> | Storage | Store at -20°C |
Physical Appearance | A solid | Shipping Condition | Evaluation sample solution : ship with blue ice.All other available size:ship with RT , or blue ice upon request |
General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months. |
SR3335 is a synthetic selective inverse agonist of RORα with Ki value of 220 nM [1][2].The retinoic acid receptor-related orphan receptor α (RORα) is an orphan receptor that plays an important role in the regulation of metabolism.SR3335 prevented the expression of endogenous RORα in HepG2. And it may suppress hepatic glucose production in type 2 diabetics. SR3335 was able to repress the expression of G6Pase. In ChIP trial, ML-176 reduced the amount of SRC2 at the G6Pase promoter [3]. In a GAL4-RORR ligand binding domain cotransfection assay, SR3335 inhibited the constitutive activity of RORα and the Ki was calculated as 220 nM [1].When treat diet-induced obese mice with SR3335 (15 mg/kg), after injected with pyruvate, the plasma glucose levels were significantly lower at each time point compared with vehicle-treated animals. The results indicated SR3335 suppressed hepatic gluconeogenesis [1].References:[1]. Naresh Kumar, Douglas J. Kojetin, et al. Identification of SR3335 (ML176): a Synthetic RORα Selective Inverse Agonist. ACS Chem Biol. 2011 March 18; 6(3): 218-222.[2]. Laura A. Solt, Thomas P. Burris. Action of RORs and their ligands in (patho)physiology. Trends in Endocrinology & Metabolism, 2012, 23(12): 619-627.[3]. Kumar N, Nuhant P, Solt LA, et al. Identification of a novel selective inverse agonist probe and analogs for the Retinoic acid receptor-related Orphan Receptor Alpha (RORα). Probe Reports from the NIH Molecular Libraries Program [Internet], Bethesda (MD): National Center for Biotechnology Information (US),2010-.2010.